PSG9
Pregnancy-specific beta-1-glycoprotein 9
Also known as: PSG11, PSG9_HUMAN, PSGII
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q00887
- Gene
- PSG9
- Ensembl
- ENSG00000183668
- Chromosome
- 19
- Canonical length
- 426 aa
- Protein class
- Plasma proteins, Predicted membrane proteins, Predicted secreted proteins
- Secretome location
- Secreted in female reproductive system
OverviewNCBI Gene
The protein encoded by this gene is a member of the pregnancy-specific glycoprotein (PSG) family. This protein family and the closely related carcinoembryonic antigen cell adhesion molecule (CEACAM) gene family are both members of the immunoglobulin superfamily, and are organized as a large gene cluster. This protein is thought to inhibit platelet-fibrinogen interactions. Several studies suggest that reduced serum concentrations of PSGs are associated with fetal growth restrictions, while up-regulation of this gene has been observed in colorectal cancers. Several pseudogenes of this gene are found on chromosome 19. Alternative splicing results in multiple transcript variants that encode multiple protein isoforms. [provided by RefSeq, Sep 2014]
Canonical amino-acid sequenceUniProt
426 residues, UniProt reviewed canonical sequence.
>Q00887|PSG9
1 MGPLPAPSCT QRITWKGLLL TASLLNFWNP PTTAEVTIEA QPPKVSEGKD VLLLVHNLPQ
61 NLPGYFWYKG EMTDLYHYII SYIVDGKIII YGPAYSGRET VYSNASLLIQ NVTRKDAGTY
121 TLHIIKRGDE TREEIRHFTF TLYLETPKPY ISSSNLNPRE AMEAVRLICD PETLDASYLW
181 WMNGQSLPVT HRLQLSKTNR TLYLFGVTKY IAGPYECEIR NPVSASRSDP VTLNLLPKLP
241 IPYITINNLN PRENKDVLAF TCEPKSENYT YIWWLNGQSL PVSPGVKRPI ENRILILPSV
301 TRNETGPYQC EIRDRYGGLR SNPVILNVLY GPDLPRIYPS FTYYRSGENL DLSCFTESNP
361 PAEYFWTING KFQQSGQKLF IPQITRNHSG LYACSVHNSA TGKEISKSMT VKVSGPCHGD
421 LTESQSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PSG9 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 100 nTPM
Expression across tissuesHPA
Tissue
- placenta: 100 nTPM
- smooth muscle: 0.7 nTPM
- colon: 0.3 nTPM
- parathyroid gland: 0.3 nTPM
- spleen: 0.3 nTPM
- bone marrow: 0.2 nTPM
Single-cell type
- syncytiotrophoblasts: 329 nCPM
- epididymal efferent duct absorptive cells: 13 nCPM
- endometrial glandular cells: 11 nCPM
- retinal bipolar cells: 9 nCPM
- extravillous trophoblasts: 7 nCPM
- adipocytes: 4.5 nCPM
Immune cell
- eosinophil: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 1.8 nTPM
- cerebral cortex: 1.2 nTPM
- amygdala: 0.9 nTPM
- white matter: 0.9 nTPM
- basal ganglia: 0.8 nTPM
- hippocampal formation: 0.8 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.85
- gnomAD pLI
- 0
- gnomAD missense Z
- -2.92
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- Fc receptor mediated inhibitory signaling pathway
- female pregnancy
- negative regulation of cytokine production involved in inflammatory response
- positive regulation of SMAD protein signal transduction
- regulation of regulatory T cell differentiation
- transforming growth factor beta receptor signaling pathway
- tolerance induction dependent upon immune response
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PSG9 as an antibody target. Whether an autoantibody or antibody against PSG9 could matter depends on whether native PSG9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PSG9 is annotated as secreted, so native PSG9 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label PSG9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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